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Kadsuric acid 3-methylester
Citing Use of our Products
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
| Size /Price /Stock |
10 mM * 1 mL in DMSO / Inquiry |
Other Packaging |
*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap |
More articles cited ChemFaces products.
Biol Pharm Bull.2018, 41(1):65-72Appl Biochem Biotechnol....2022...Food Chem.2020, 332:127412Molecules.2020, 25(23):5609. Process Biochemistry2019, 85:106-115Biosci Biotechnol Biochem....2021...Oxid Med Cell Longev....2020...Chemistry of Natural Compounds...2019...
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Kadsuric acid 3-methylester
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ACS Chem Biol.2019, 14(5):873-881Front Pharmacol.2021, 12:762829. Jour. of Stored Pro & Postharvest Res.2016, 7(3):32-36Sci Rep.2019, 9(1):6429J Ethnopharmacol.2022, 282:114574. Biorxiv.2020, doi: 10.1101.ACS Pharmacol. Transl. Sci.2022, 5,7,479-490Antioxidants (Basel).2021, 10(8):1300. J Ethnopharmacol.2017, 209:305-316Appl Microbiol Biotechnol.2018, 102(12):5105-5120
Related Screening Libraries
| Size /Price /Stock |
10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
|
Related Libraries |
Triterpenoids Compound Library |
| Description: |
Kadsuric acid 3-methylester is a natural product from Kadsura longipedunculata Finet.et Gagnep. |
Kadsuric acid 3-methylester Description
| Source: |
The herbs of Kadsura longipedunculata Finet.et Gagnep |
| Solvent: |
Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc. |
| Storage: |
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
|
| After receiving: |
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling. |
ChemFaces New Products and Compounds
Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals
Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)PMID: 29328914
Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)PMID: 32004475
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)PMID: 29149595
ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)PMID: 29553709
Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.
IF=13.297(2019)PMID: 28005066
Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
| 1 mM |
2.0631 mL |
10.3157 mL |
20.6313 mL |
41.2626 mL |
51.5783 mL |
| 5 mM |
0.4126 mL |
2.0631 mL |
4.1263 mL |
8.2525 mL |
10.3157 mL |
| 10 mM |
0.2063 mL |
1.0316 mL |
2.0631 mL |
4.1263 mL |
5.1578 mL |
| 50 mM |
0.0413 mL |
0.2063 mL |
0.4126 mL |
0.8253 mL |
1.0316 mL |
| 100 mM |
0.0206 mL |
0.1032 mL |
0.2063 mL |
0.4126 mL |
0.5158 mL |
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
| Structure Identification: |
| Helvetica Chimica Acta, 2010 , 91 (5) :856-861. | | Terpenoids from Two Dicranopteris Species[Reference: WebLink] |
METHODS AND RESULTS:
Two new compounds, (6S,13S)-6-{[β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}cleroda-3,14-dien-13-ol (1) and Kadsuric acid 3-methylester (2), together with nine known compounds, (6S,13E)-6-{[β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}cleroda-3,13-dien-15-ol (3), (6S,13S)-6-[6-O-acetyl-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}-13-{[α-L-rhamnopyranosyl-(1→4)-β-D-fucopyranosyl]oxy}cleroda-3,14-diene (4), (6S,13S)-6-{[6-O-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}-13-{[α-L-rhamnopyranosyl-(1→4)-β-D-fucopyranosyl]oxy}cleroda-3,14-diene (5), 15-hydroxydehydroabietic acid (6), 15-hydroxylabd-8(17)-en-19-oic acid (7), junicedric acid (8), (4β)-kaur-16-en-18-oic acid (9), (4β)-16-hydroxykauran-18-oic acid (10), and (4β,16β)-16-hydroxykauran-18-oic acid (11) were isolated from the fronds of Dicranopteris linearis or D. ampla.
CONCLUSIONS:
Their structures were established by extensive 1D- and 2D-NMR spectroscopy. Compounds 1 and 3–8 showed no anti-HIV activities. |
|
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